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PACBAR for Comprehensive Capture and Delineation of Proanthocyanidin Structures

Journal of agricultural and food chemistry, 2020-11, Vol.68 (47), p.13541-13549

2020

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Effects of feeding Lespedeza cuneata pellets with Medicago sativa hay to sheep: Nutritional impact, characterization and degradation of condensed tannin during digestion

Animal feed science and technology, 2018-11, Vol.245, p.41-47

2018

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ChemInform Abstract: Synthesis of (+)- and (-)-Phaselic Acid

ChemInform, 2013-07, Vol.44 (30), p.no-no

Zeller, Wayne E.

2013

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1H–13C HSQC NMR Spectroscopy for Estimating Procyanidin/Prodelphinidin and cis/trans-Flavan-3-ol Ratios of Condensed Tannin Samples: Correlation with Thiolysis

Journal of agricultural and food chemistry, 2015-02, Vol.63 (7), p.1967-1973

2015

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1 H– 13 C HSQC NMR Spectroscopy for Estimating Procyanidin/Prodelphinidin and cis / trans -Flavan-3-ol Ratios of Condensed Tannin Samples: Correlation with Thiolysis

Journal of agricultural and food chemistry, 2015-02, Vol.63 (7), p.1967-1973

2015

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CMR Spectra of N-Oxygenated Pyrazoles. I. 3,5-Dialkyl- and 3-Alkyl-5-phenyl-4-oxo-4H-pyrazole 1,2-Dioxides

Heterocycles, 1999, Vol.51 (1), p.145

1999

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H-¹³C HSQC NMR spectroscopy for estimating procyanidin/prodelphinidin and cis/trans-flavan-3-ol ratios of condensed tannin samples: correlation with thiolysis

Journal of agricultural and food chemistry, 2015-02, Vol.63 (7), p.1967-1973

2015

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Challenges in Analyzing Bioactive Proanthocyanidins

Recent Advances in Polyphenol Research, Volume 7, 2021

2021

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Hypocholesteremic agent compactin (ML-236B). Total synthesis of the hexahydronaphthalene portion

Journal of organic chemistry, 1982-01, Vol.47 (1), p.180-182

1982

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DIC-Mediated Coupling of Carboxylic Acids to (4R, 5S)-4-Methyl-5-Phenyl-2-Oxazolidinone

Synthetic communications, 2000-04, Vol.30 (7), p.1221-1226

2000

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Hypocholesterolemic agent compactin. an alternative diels-alder strategy for the synthesis of the hexahydronaphthalene portion

Tetrahedron letters, 1984, Vol.25 (16), p.1655-1658

1984

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ChemInform Abstract: DIC-Mediated Coupling of Carboxylic Acids to (4R,5S)-4-Methyl-5-phenyl-2-oxazolidinone

ChemInform, 2000-08, Vol.31 (33), p.no-no

2000

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Editor's Choice – Recommendations for Registry Data Collection for Revascularisations of Acute Limb Ischaemia: A Delphi Consensus from the International Consortium of Vascular Registries

European journal of vascular and endovascular surgery, 2019-06, Vol.57 (6), p.816-821

2019

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Antagonists of the EP3 Receptor for Prostaglandin E2 Are Novel Antiplatelet Agents That Do Not Prolong Bleeding

ACS chemical biology, 2009-02, Vol.4 (2), p.115-126

2009

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Development of a Scalable Process for DG-041, a Potent EP3 Receptor Antagonist, via Tandem Heck Reactions

Organic process research & development, 2007-07, Vol.11 (4), p.747-753

2007

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3,4-Disubstituted indole acylsulfonamides : A novel series of potent and selective human EP3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (1), p.123-126

2009

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Peri-substituted hexahydro-indolones as novel, potent and selective human EP3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (3), p.778-782

2009

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3-Acrylamide-4-aryloxyindoles: synthesis, biological evaluation and metabolic stability of potent and selective EP3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1528-1531

2009

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Heterocyclic 1,7-disubstituted indole sulfonamides are potent and selective human EP3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-12, Vol.19 (23), p.6797-6800

2009

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Peri-substituted hexahydro-indolones as novel, potent and selective human EP 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (3), p.778-782

2009

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3,4-Disubstituted indole acylsulfonamides: A novel series of potent and selective human EP sub(3) receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (1), p.123-126

2009

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Heterocyclic 1,7-disubstituted indole sulfonamides are potent and selective human EP 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (23), p.6797-6800

2009

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PACBAR for Comprehensive Capture and Delineation of Proanthocyanidin Structures

Effects of feeding Lespedeza cuneata pellets with Medicago sativa hay to sheep: Nutritional impact, characterization and degradation of condensed tannin during digestion

ChemInform Abstract: Synthesis of (+)- and (-)-Phaselic Acid

1H–13C HSQC NMR Spectroscopy for Estimating Procyanidin/Prodelphinidin and cis/trans-Flavan-3-ol Ratios of Condensed Tannin Samples: Correlation with Thiolysis

1 H– 13 C HSQC NMR Spectroscopy for Estimating Procyanidin/Prodelphinidin and cis / trans -Flavan-3-ol Ratios of Condensed Tannin Samples: Correlation with Thiolysis

CMR Spectra of N-Oxygenated Pyrazoles. I. 3,5-Dialkyl- and 3-Alkyl-5-phenyl-4-oxo-4H-pyrazole 1,2-Dioxides

H-¹³C HSQC NMR spectroscopy for estimating procyanidin/prodelphinidin and cis/trans-flavan-3-ol ratios of condensed tannin samples: correlation with thiolysis

Challenges in Analyzing Bioactive Proanthocyanidins

Hypocholesteremic agent compactin (ML-236B). Total synthesis of the hexahydronaphthalene portion

DIC-Mediated Coupling of Carboxylic Acids to (4R, 5S)-4-Methyl-5-Phenyl-2-Oxazolidinone

Hypocholesterolemic agent compactin. an alternative diels-alder strategy for the synthesis of the hexahydronaphthalene portion

ChemInform Abstract: DIC-Mediated Coupling of Carboxylic Acids to (4R,5S)-4-Methyl-5-phenyl-2-oxazolidinone

Editor's Choice – Recommendations for Registry Data Collection for Revascularisations of Acute Limb Ischaemia: A Delphi Consensus from the International Consortium of Vascular Registries

Antagonists of the EP3 Receptor for Prostaglandin E2 Are Novel Antiplatelet Agents That Do Not Prolong Bleeding

Development of a Scalable Process for DG-041, a Potent EP3 Receptor Antagonist, via Tandem Heck Reactions

3,4-Disubstituted indole acylsulfonamides : A novel series of potent and selective human EP3 receptor antagonists

Peri-substituted hexahydro-indolones as novel, potent and selective human EP3 receptor antagonists

3-Acrylamide-4-aryloxyindoles: synthesis, biological evaluation and metabolic stability of potent and selective EP3 receptor antagonists

Heterocyclic 1,7-disubstituted indole sulfonamides are potent and selective human EP3 receptor antagonists

Peri-substituted hexahydro-indolones as novel, potent and selective human EP 3 receptor antagonists

3,4-Disubstituted indole acylsulfonamides: A novel series of potent and selective human EP sub(3) receptor antagonists

Heterocyclic 1,7-disubstituted indole sulfonamides are potent and selective human EP 3 receptor antagonists

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